Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_assertion description "[Chd7(COA1/+) mice phenocopied human CHARGE syndrome and displayed developmental defects in the telencephalic midline, including dilated third and lateral ventricles, reduced cerebral cortex, and corpus callosum crossing failure.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_assertion evidence source_evidence_literature NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_assertion SIO_000772 22658483 NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_assertion wasDerivedFrom befree-2016 NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_assertion wasGeneratedBy ECO_0000203 NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP986574.RA2RTvABjdvGVproTUz9ydp4KfrJrkPlRtxl6l1UKkECQ130_provenance.